Evidence map›Paper›PMID 24655566›Full record

ArticleBMC neurology2014

CD58 polymorphisms associated with the risk of neuromyelitis optica in a Korean population.

Jason Yongha Kim, Joon Seol Bae, Ho Jin Kim, Hyoung Doo Shin

Open access · goldAbstract read
In one paragraph

Article in BMC neurology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.9field-weighted citation impact, top 16% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

17 citing papers in PubMed, 30 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Interaction of HLA Class II rs9272219 andFrontiers in genetics · 2021
    Article
  6. CD58 Immunobiology at a Glance.Frontiers in immunology · 2021
    Review
  7. Article
  8. Association ofAuto- immunity highlights · 2019
    Article
  9. Article
  10. Association ofNeural regeneration research · 2019
    Article
  11. Pediatric Neuromyelitis Optica Spectrum Disorders.Current treatment options in neurology · 2018
    Review
  12. Association of Optic Neuritis withJournal of ophthalmology · 2018
    Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Roles of CD48 in regulating immunity and tolerance.Clinical immunology (Orlando, Fla.) · 2016
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors at 4 institutions in 1 country.

Jason Yongha Kim
Joon Seol Bae
Ho Jin Kim
Hyoung Doo ShinDepartment of Life Science, Sogang University, 1 Shinsu-dong, Seoul 121-742, Republic of Korea. hdshin@sogang.ac.kr.
National Cancer Center · KRSamsung Medical Center · KRSNP Genetics (South Korea) · KRSogang University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNeuromyelitis optica (NMO) is a serious inflammatory demyelinating disease (IDD), characterized by the inflammation and demyelination of optic nerves and spinal cords, which subsequently leads to the loss of function. In a previous genome-wide association study, cluster of differentiation 58 (CD58) region was found to be susceptible for the risk of multiple sclerosis (MS) in Caucasian, and the association between CD58 variants and MS was replicated in Americans. However, no study has been conducted to explore the possible association between CD58 and NMO yet. Thus, this study aimed to investigate the association of CD58 polymorphisms with the risk of NMO in a Korean population.

methodsUsing TaqMan assay, 6 single nucleotide polymorphisms (SNPs) were genotyped in 98 NMO patients and 237 normal controls (N = 336). Logistic regression analysis was conducted to find a possible association between CD58 polymorphisms and NMO.

resultsThe analysis results showed that 6 variations (rs2300747, rs1335532, rs12044852, rs1016140, CD58_ht1, and CD58_ht3) showed significant associations (P = 0.002 ~ 0.008, P(corr) = 0.01 ~ 0.04).

conclusionThe genetic variations in CD58 may be associated with the susceptibility of NMO in a Korean population. Based on previous studies, we suspect that the A allele of rs2300747 may decrease CD58 RNA expression, thus increasing NMO risk. Also, we deduced that the G allele of rs1016140 caused an increase of T cell activity, which in turn eased the access of AQP4 antibody into central nervous system (CNS) and ultimately leading to NMO development.

Indexed as

Population SurveillanceAdolescentAdultAgedCD58 AntigensChildFemaleGenetic Association StudiesHumansMaleMiddle AgedNeuromyelitis OpticaPolymorphism, Single NucleotideRepublic of KoreaRisk FactorsYoung AdultCD58 Antigens

Identifiers

PMID24655566
PMCPMC3998011
OpenAlexW2005855288

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.